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Article: An H5N1 M2e-based multiple antigenic peptide vaccine confers heterosubtypic protection from lethal infection with pandemic 2009 H1N1 virus
Title | An H5N1 M2e-based multiple antigenic peptide vaccine confers heterosubtypic protection from lethal infection with pandemic 2009 H1N1 virus | ||||||||||
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Authors | |||||||||||
Issue Date | 2010 | ||||||||||
Publisher | BioMed Central Ltd. The Journal's web site is located at http://www.virologyj.com/home/ | ||||||||||
Citation | Virology Journal, 2010, v. 7 How to Cite? | ||||||||||
Abstract | Background. A 2009 global influenza pandemic caused by a novel swine-origin H1N1 influenza A virus has posted an increasing threat of a potential pandemic by the highly pathogenic avian influenza (HPAI) H5N1 virus, driving us to develop an influenza vaccine which confers cross-protection against both H5N1 and H1N1 viruses. Previously, we have shown that a tetra-branched multiple antigenic peptide (MAP) vaccine based on the extracellular domain of M2 protein (M2e) from H5N1 virus (H5N1-M2e-MAP) induced strong immune responses and cross-protection against different clades of HPAI H5N1 viruses. In this report, we investigated whether such M2e-MAP presenting the H5N1-M2e consensus sequence can afford heterosubtypic protection from lethal challenge with the pandemic 2009 H1N1 virus. Results. Our results demonstrated that H5N1-M2e-MAP plus Freund's or aluminum adjuvant induced strong cross-reactive IgG antibody responses against M2e of the pandemic H1N1 virus which contains one amino acid variation with M2e of H5N1 at position 13. These cross-reactive antibodies may maintain for 6 months and bounced back quickly to the previous high level after the 2nd boost administered 2 weeks before virus challenge. H5N1-M2e-MAP could afford heterosubtypic protection against lethal challenge with pandemic H1N1 virus, showing significant decrease of viral replications and obvious alleviation of histopathological damages in the challenged mouse lungs. 100% and 80% of the H5N1-M2e-MAP-vaccinated mice with Freund's and aluminum adjuvant, respectively, survived the lethal challenge with pandemic H1N1 virus. Conclusions. Our results suggest that H5N1-M2e-MAP has a great potential to prevent the threat from re-emergence of pandemic H1N1 influenza and possible novel influenza pandemic due to the reassortment of HPAI H5N1 virus with the 2009 swine-origin H1N1 influenza virus. © 2010 Zhao et al; licensee BioMed Central Ltd. | ||||||||||
Persistent Identifier | http://hdl.handle.net/10722/135277 | ||||||||||
ISSN | 2023 Impact Factor: 4.0 2023 SCImago Journal Rankings: 1.016 | ||||||||||
PubMed Central ID | |||||||||||
ISI Accession Number ID |
Funding Information: This study was supported by Natural Science Foundation of China (30901371), Mega-projects of Science Research for the 11th Five-Year Plan (2009ZX10004-401), National Basic Research Program of China (973 Program, 2005CB523001), and National Science and Technology Infrastructure Program (2006BA06A15). | ||||||||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Zhao, G | en_HK |
dc.contributor.author | Sun, S | en_HK |
dc.contributor.author | Du, L | en_HK |
dc.contributor.author | Xiao, W | en_HK |
dc.contributor.author | Ru, Z | en_HK |
dc.contributor.author | Kou, Z | en_HK |
dc.contributor.author | Guo, Y | en_HK |
dc.contributor.author | Yu, H | en_HK |
dc.contributor.author | Jiang, S | en_HK |
dc.contributor.author | Lone, Y | en_HK |
dc.contributor.author | Zheng, BJ | en_HK |
dc.contributor.author | Zhou, Y | en_HK |
dc.date.accessioned | 2011-07-27T01:31:05Z | - |
dc.date.available | 2011-07-27T01:31:05Z | - |
dc.date.issued | 2010 | en_HK |
dc.identifier.citation | Virology Journal, 2010, v. 7 | en_HK |
dc.identifier.issn | 1743-422X | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/135277 | - |
dc.description.abstract | Background. A 2009 global influenza pandemic caused by a novel swine-origin H1N1 influenza A virus has posted an increasing threat of a potential pandemic by the highly pathogenic avian influenza (HPAI) H5N1 virus, driving us to develop an influenza vaccine which confers cross-protection against both H5N1 and H1N1 viruses. Previously, we have shown that a tetra-branched multiple antigenic peptide (MAP) vaccine based on the extracellular domain of M2 protein (M2e) from H5N1 virus (H5N1-M2e-MAP) induced strong immune responses and cross-protection against different clades of HPAI H5N1 viruses. In this report, we investigated whether such M2e-MAP presenting the H5N1-M2e consensus sequence can afford heterosubtypic protection from lethal challenge with the pandemic 2009 H1N1 virus. Results. Our results demonstrated that H5N1-M2e-MAP plus Freund's or aluminum adjuvant induced strong cross-reactive IgG antibody responses against M2e of the pandemic H1N1 virus which contains one amino acid variation with M2e of H5N1 at position 13. These cross-reactive antibodies may maintain for 6 months and bounced back quickly to the previous high level after the 2nd boost administered 2 weeks before virus challenge. H5N1-M2e-MAP could afford heterosubtypic protection against lethal challenge with pandemic H1N1 virus, showing significant decrease of viral replications and obvious alleviation of histopathological damages in the challenged mouse lungs. 100% and 80% of the H5N1-M2e-MAP-vaccinated mice with Freund's and aluminum adjuvant, respectively, survived the lethal challenge with pandemic H1N1 virus. Conclusions. Our results suggest that H5N1-M2e-MAP has a great potential to prevent the threat from re-emergence of pandemic H1N1 influenza and possible novel influenza pandemic due to the reassortment of HPAI H5N1 virus with the 2009 swine-origin H1N1 influenza virus. © 2010 Zhao et al; licensee BioMed Central Ltd. | en_HK |
dc.language | eng | en_US |
dc.publisher | BioMed Central Ltd. The Journal's web site is located at http://www.virologyj.com/home/ | en_HK |
dc.relation.ispartof | Virology Journal | en_HK |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.rights | Virology Journal. Copyright © BioMed Central Ltd. | - |
dc.subject.mesh | Cross Protection | - |
dc.subject.mesh | Disease Outbreaks | - |
dc.subject.mesh | Influenza Vaccines - administration and dosage - immunology | - |
dc.subject.mesh | Influenza, Human - epidemiology - immunology - prevention and control - virology | - |
dc.subject.mesh | Viral Matrix Proteins - administration and dosage - chemistry - immunology | - |
dc.title | An H5N1 M2e-based multiple antigenic peptide vaccine confers heterosubtypic protection from lethal infection with pandemic 2009 H1N1 virus | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Zheng, BJ:bzheng@hkucc.hku.hk | en_HK |
dc.identifier.authority | Zheng, BJ=rp00353 | en_HK |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1186/1743-422X-7-151 | en_HK |
dc.identifier.pmid | 20624292 | - |
dc.identifier.pmcid | PMC2912260 | - |
dc.identifier.scopus | eid_2-s2.0-77954409486 | en_HK |
dc.identifier.hkuros | 188635 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-77954409486&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 7 | en_HK |
dc.identifier.isi | WOS:000282601300001 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Zhao, G=8684553000 | en_HK |
dc.identifier.scopusauthorid | Sun, S=35171536200 | en_HK |
dc.identifier.scopusauthorid | Du, L=8686996200 | en_HK |
dc.identifier.scopusauthorid | Xiao, W=9245533300 | en_HK |
dc.identifier.scopusauthorid | Ru, Z=36197231500 | en_HK |
dc.identifier.scopusauthorid | Kou, Z=23034818200 | en_HK |
dc.identifier.scopusauthorid | Guo, Y=8555122500 | en_HK |
dc.identifier.scopusauthorid | Yu, H=36349449900 | en_HK |
dc.identifier.scopusauthorid | Jiang, S=7404453146 | en_HK |
dc.identifier.scopusauthorid | Lone, Y=36196779400 | en_HK |
dc.identifier.scopusauthorid | Zheng, BJ=7201780588 | en_HK |
dc.identifier.scopusauthorid | Zhou, Y=8791655300 | en_HK |
dc.identifier.citeulike | 7493888 | - |
dc.identifier.issnl | 1743-422X | - |